These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

95 related articles for article (PubMed ID: 27236536)

  • 1. Moyamoya syndrome and 6p chromosome rearrangements: Expanding evidences of a new association.
    Toldo I; Po' C; Morao V; Talenti G; Causin F; D'Avella D; Tenconi R; Suppiej A; Sartori S
    Eur J Paediatr Neurol; 2016 Sep; 20(5):766-71. PubMed ID: 27236536
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Complex chromosome rearrangement of 6p25.3->p23 and 12q24.32->qter in a child with moyamoya.
    Rosenberg RE; Egan M; Rodgers S; Harter D; Burnside RD; Milla S; Pappas J
    Pediatrics; 2013 Jun; 131(6):e1996-2001. PubMed ID: 23713105
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Microduplication of 15q13.3 and Microdeletion of 18q21.32 in a Patient with Moyamoya Syndrome.
    Luisa SF; Rizzo A; Bedini G; Capone F; Di Lazzaro V; Nava S; Acerbi F; Rossi DS; Binelli S; Faragò G; Gioppo A; Grisoli M; Bruzzone MG; Ferroli P; Pantaleoni C; Caputi L; Gomez JV; Parati EA; Bersano A
    Int J Mol Sci; 2018 Nov; 19(11):. PubMed ID: 30463371
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Karyotype-phenotype correlation in partial trisomies of the short arm of chromosome 6: a family case report and review of the literature.
    Castiglione A; Guaran V; Astolfi L; Orioli E; Zeri G; Gemmati D; Bovo R; Montaldi A; Alghisi A; Martini A
    Cytogenet Genome Res; 2013; 141(4):243-59. PubMed ID: 23942271
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the Literature.
    Prontera P; Rogaia D; Mencarelli A; Ottaviani V; Sallicandro E; Guercini G; Esposito S; Bersano A; Merla G; Stangoni G
    Int J Mol Sci; 2017 Sep; 18(9):. PubMed ID: 28926972
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Loss of BRCC3 deubiquitinating enzyme leads to abnormal angiogenesis and is associated with syndromic moyamoya.
    Miskinyte S; Butler MG; Hervé D; Sarret C; Nicolino M; Petralia JD; Bergametti F; Arnould M; Pham VN; Gore AV; Spengos K; Gazal S; Woimant F; Steinberg GK; Weinstein BM; Tournier-Lasserve E
    Am J Hum Genet; 2011 Jun; 88(6):718-728. PubMed ID: 21596366
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ophthalmological Findings in 6p Deletion Syndrome.
    Cornelis T; Rayyan M; Devriendt K; Casteels I
    Ophthalmic Genet; 2015 Jun; 36(2):165-7. PubMed ID: 25675350
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A case of CHOPS syndrome accompanied with moyamoya disease and systemic vasculopathy.
    Kim SY; Kim MJ; Kim SJ; Lee JE; Chae JH; Ko JM
    Brain Dev; 2021 Mar; 43(3):454-458. PubMed ID: 33248856
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Identification of an association between Robinow syndrome and moyamoya.
    Qaiser R; Scott RM; Smith ER
    Pediatr Neurosurg; 2009; 45(1):69-72. PubMed ID: 19258733
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [No association between moyamoya disease and polymorphism of IGF2R].
    Yamamoto T; Akasaka Y; Ohtani K; Hayashi T; Kashiwagi S; Ichiyama T; Nishikawa M; Kato M; Maegaki Y; Oka A; Ohno K
    No To Hattatsu; 2005 Jan; 37(1):15-9. PubMed ID: 15675354
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Linkage analysis of moyamoya disease on chromosome 6.
    Inoue TK; Ikezaki K; Sasazuki T; Matsushima T; Fukui M
    J Child Neurol; 2000 Mar; 15(3):179-82. PubMed ID: 10757474
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Refined genotype-phenotype correlations in cases of chromosome 6p deletion syndromes.
    Mirza G; Williams RR; Mohammed S; Clark R; Newbury-Ecob R; Baldinger S; Flinter F; Ragoussis J
    Eur J Hum Genet; 2004 Sep; 12(9):718-28. PubMed ID: 15150541
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Deletion of the long arm of chromosome 6: report on a new case with intractable epilepsy.
    Cerminara C; Bombardieri R; Pinci M; Seri S; Curatolo P
    J Child Neurol; 2006 Jun; 21(6):527-31. PubMed ID: 16948941
    [TBL] [Abstract][Full Text] [Related]  

  • 14. De novo mutations in CBL causing early-onset paediatric moyamoya angiopathy.
    Guey S; Grangeon L; Brunelle F; Bergametti F; Amiel J; Lyonnet S; Delaforge A; Arnould M; Desnous B; Bellesme C; Hervé D; Schwitalla JC; Kraemer M; Tournier-Lasserve E; Kossorotoff M
    J Med Genet; 2017 Aug; 54(8):550-557. PubMed ID: 28343148
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairment.
    Anderlid BM; Schoumans J; Hallqvist A; Ståhl Y; Wallin A; Blennow E; Nordenskjöld M
    Eur J Hum Genet; 2003 Jan; 11(1):89-92. PubMed ID: 12529712
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Management of moyamoya syndrome in patients with Noonan syndrome.
    Gupta M; Choudhri OA; Feroze AH; Do HM; Grant GA; Steinberg GK
    J Clin Neurosci; 2016 Jun; 28():107-11. PubMed ID: 26778511
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Moyamoya syndrome in a child with Noonan syndrome.
    Hung PC; Wang HS; Wong AM
    Pediatr Neurol; 2011 Aug; 45(2):129-31. PubMed ID: 21763956
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genomic gain at 6p21: a new cryptic molecular rearrangement in secondary myelodysplastic syndrome and acute myeloid leukemia.
    La Starza R; Aventin A; Matteucci C; Crescenzi B; Romoli S; Testoni N; Pierini V; Ciolli S; Sambani C; Locasciulli A; Di Bona E; Lafage-Pochitaloff M; Martelli MF; Marynen P; Mecucci C
    Leukemia; 2006 Jun; 20(6):958-64. PubMed ID: 16617324
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Early onset of moyamoya syndrome in a Down syndrome patient with the genetic variant RNF213 p.R4810K.
    Chong PF; Ogata R; Kobayashi H; Koizumi A; Kira R
    Brain Dev; 2015 Sep; 37(8):822-4. PubMed ID: 25547042
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Down syndrome and moyamoya: clinical presentation and surgical management.
    See AP; Ropper AE; Underberg DL; Robertson RL; Scott RM; Smith ER
    J Neurosurg Pediatr; 2015 Jul; 16(1):58-63. PubMed ID: 25837890
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.